List of variants in gene LRP2 reported as likely benign by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 45

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004525.3(LRP2):c.63G>C (p.Ala21=)	rs1559014	0.99771
NM_004525.3(LRP2):c.12280A>G (p.Lys4094Glu)	rs2075252	0.79497
NM_004525.3(LRP2):c.2025C>T (p.Val675=)	rs830994	0.61350
NM_004525.3(LRP2):c.12628A>C (p.Ile4210Leu)	rs4667591	0.60691
NM_004525.3(LRP2):c.13113C>T (p.Ile4371=)	rs990626	0.59977
NM_004525.3(LRP2):c.2460A>G (p.Thr820=)	rs2241190	0.54408
NM_004525.3(LRP2):c.3069A>G (p.Thr1023=)	rs831043	0.53755
NM_004525.3(LRP2):c.3660A>G (p.Ala1220=)	rs831042	0.50520
NM_004525.3(LRP2):c.10503G>A (p.Gln3501=)	rs2229265	0.45093
NM_004525.3(LRP2):c.3054C>A (p.Thr1018=)	rs2075249	0.41290
NM_004525.3(LRP2):c.4875T>C (p.Cys1625=)	rs2229267	0.38704
NM_004525.3(LRP2):c.248A>G (p.Asn83Ser)	rs2229263	0.33289
NM_004525.3(LRP2):c.639C>T (p.Asp213=)	rs2229266	0.30270
NM_004525.3(LRP2):c.8614G>A (p.Ala2872Thr)	rs2228171	0.25207
NM_004525.3(LRP2):c.5100C>T (p.Ser1700=)	rs2302694	0.19156
NM_004525.3(LRP2):c.5859A>G (p.Arg1953=)	rs11886219	0.16510
NM_004525.3(LRP2):c.11601T>C (p.Cys3867=)	rs2229268	0.15380
NM_004525.3(LRP2):c.7626C>G (p.Arg2542=)	rs13397109	0.12249
NM_004525.3(LRP2):c.2376T>C (p.Asp792=)	rs33954745	0.09210
NM_004525.3(LRP2):c.6759T>C (p.Asp2253=)	rs35114151	0.04805
NM_004525.3(LRP2):c.4236G>C (p.Arg1412=)	rs34915742	0.04398
NM_004525.3(LRP2):c.4046-6T>C	rs76714416	0.04392
NM_004525.3(LRP2):c.13155C>T (p.His4385=)	rs16856476	0.04079
NM_004525.3(LRP2):c.3836A>C (p.Asp1279Ala)	rs17848149	0.03848
NM_004525.3(LRP2):c.7894A>G (p.Asn2632Asp)	rs17848169	0.02788
NM_004525.3(LRP2):c.12151+4T>C	rs17848192	0.02665
NM_004525.3(LRP2):c.2006G>A (p.Gly669Asp)	rs34291900	0.02496
NM_004525.3(LRP2):c.6045C>T (p.Ala2015=)	rs34834388	0.01962
NM_004525.3(LRP2):c.4344C>G (p.Ala1448=)	rs35297090	0.01784
NM_004525.3(LRP2):c.11759-5T>G	rs76488092	0.01524
NM_004525.3(LRP2):c.3452C>T (p.Pro1151Leu)	rs150552608	0.01319
NM_004525.3(LRP2):c.13250G>A (p.Gly4417Asp)	rs41268685	0.01191
NM_004525.3(LRP2):c.13134C>G (p.Pro4378=)	rs73970129	0.01063
NM_004525.3(LRP2):c.10804G>A (p.Ala3602Thr)	rs144081819	0.01045
NM_004525.3(LRP2):c.9033-8T>C	rs140148483	0.01021
NM_004525.3(LRP2):c.5085G>A (p.Ser1695=)	rs145384264	0.00999
NM_004525.3(LRP2):c.1172-8G>A	rs115371758	0.00955
NM_004525.3(LRP2):c.1167T>G (p.Asp389Glu)	rs111704488	0.00952
NM_004525.3(LRP2):c.11996T>G (p.Val3999Gly)	rs79723119	0.00834
NM_004525.3(LRP2):c.2175C>T (p.Thr725=)	rs141180155	0.00820
NM_004525.3(LRP2):c.11092G>A (p.Val3698Met)	rs34355135	0.00560
NM_004525.3(LRP2):c.92C>T (p.Ala31Val)	rs144829356	0.00280
NM_004525.3(LRP2):c.10165A>G (p.Ile3389Val)	rs140272085	0.00055
NM_004525.3(LRP2):c.402C>A (p.Pro134=)	rs34104660
NM_004525.3(LRP2):c.775G>C (p.Gly259Arg)	rs34693334

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.